A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595811



Internal ID16036534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:159102928..159104226hg38UCSC Ensembl
Innerchr4:160024080..160025378hg19UCSC Ensembl
Innerchr4:160243530..160244828hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1009765
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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